FDA.reportPublic FDA data

altor Safety Hand Sanitizer Gel

Manufacturer
Altor Safety | Aero Healthcare
Effective date
2021-02-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:53:29

Label at a glance#

Productaltor Safety Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children under 6 years of age should be supervised when suing this product

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable-Keep away from fire or flame

For external use only

stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

irritation or rash appears and lasts

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact a poison control center right away.

When using this product

OTC - DO NOT USE SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly cover your hands

Rub hands together briskly until dry

Children under 6 years of age should be supervised when suing this product

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, C10-30 Alkyl Acrylate Crosspolymer, Isopropyl Alcohol, Methyl Gluceth-20, Trimethylene Glycol, Tocopheryl Acetate, Aloe Barbendensis Leaf Juice, Aminomethyl Propanol

Other Information

OTHER SAFETY INFORMATION

Store Below 140 °F (40ºC)

May discolor certain fabrics or surfaces

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Altor_16ozAltor_16ozAltor 8ozAltor 8ozACG3785-085 _1 GalACG3785-085 _1 Gal

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81248-08581248-085-01, 81248-085-02, 81248-085-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
METHYL GLUCETH-20J3QD0LD11PIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
PROPANEDIOL5965N8W85TIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
ISOPROPYL ALCOHOLND2M416302IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ddcefa9a-add5-7c0c-e053-2a95a90af550b69799e5-4513-97af-e053-2995a90abc1b2022-04-29WarningsExact identifier
spl set id: b69799e5-4513-97af-e053-2995a90abc1b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.